HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1787004Generated: October 31, 2026
N-methyl-2-pyrrolidone → HCID 67520732, compound
https://huagongshe.com/reaction/1787004
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Reactant | Pyridinium chloride | HCID 10176127 | — |
| Reactant | HCID 28401833 | HCID 28401833 | — |
| Reactant | HCID 67521136 | HCID 67521136 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 67520732 | HCID 67520732 | 91.8% |
Reaction Steps
A mixture of 4-phenoxy-6,7-dihydro-9H-pyrimido[4′,5′:4,5]pyrrolo[2,1-c][1,4]oxazine (69 mg), 3-(4-amino-2-chlorophenoxy)benzonitrile (95 mg), pyridine hydrochloride (75 mg) and 1-methyl-2-pyrrolidone (1 mL) was stirred at 140° C. for 14 hrs. After the completion of the reaction, the mixture was diluted with ethyl acetate and washed with saturated aqueous sodium hydrogen carbonate and saturated brine. The organic layer was dried over magnesium sulfate. After concentration under reduced pressure, the residue was subjected to silica gel column chromatography (hexane/ethyl acetate=50/50→0/100). The obtained fractions were collected and concentrated, and the residue was dissolved in ethyl acetate (2 mL) and treated with 4N hydrochloric acid/ethyl acetate (0.13 mL) to give the title compound (81 mg) as hydrochloride crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07507740B2 |
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| Source dataset | uspto-grants-2009_03 |
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| ORD ID | ord-f54fe403840b4db7bc828ad07e9330b7 |
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| Source note | uspto-grants-2009_03 |
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